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dc.contributor.authorN. Chaichanaen_US
dc.contributor.authorS. Dheeranupattanaen_US
dc.contributor.authorA. Jatisatienren_US
dc.contributor.authorS. Wangkarnen_US
dc.date.accessioned2018-09-04T04:03:38Z-
dc.date.available2018-09-04T04:03:38Z-
dc.date.issued2011-12-13en_US
dc.identifier.issn18125679en_US
dc.identifier.issn16823974en_US
dc.identifier.other2-s2.0-83055197119en_US
dc.identifier.other10.3923/ajps.2011.338.341en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=83055197119&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/49528-
dc.description.abstractPlant propagation through tissue culture technique is required to produce plant secondaiy metabolite. The objective of this experiment was to obtain the optimum media composition for in vitro shoot and root formation of Stemona sp. It was shown that Murashige and Skoog (MS) medium supplement with 3 mg L _1 benzyladenine and half-MS medium supplemented with 2 mg L _1 indolebutyric acid were the appropriate media for shoot and root induction, respectively. The media could produce 100% of shoot induction and 80% of root induction. The increase or decrease in r,2'-didehydrostemofoline was related to the root growth. The highest 12'-didehydrostemofoline production of 31.04 mg g _1 root diy weight was observed in 16 week old root. © 2011 Asian Network for Scientific Information.en_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.titleMicro-propagation and 1'2'-didehydrostemofoline production from stemona spen_US
dc.typeJournalen_US
article.title.sourcetitleAsian Journal of Plant Sciencesen_US
article.volume10en_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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